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首页> 外文期刊>Tropical Journal of Pharmaceutical Research >Bioadhesive controlled release clotrimazole vaginal tablets
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Bioadhesive controlled release clotrimazole vaginal tablets

机译:生物粘附控制释放克霉唑阴道片

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Purpose: To formulate bioadhesive clotrimazole vaginal tablets using natural polymers in order to provide long-term therapeutic action at the site of infection. Methods: The tablets were prepared by direct compression using bioadhesive polymer mixtures: hydroxypropyl methylcellulose/sodium carboxymethylcellulose (HPMC/NaCMC) and HPMC/Guar gum (GG) in different ratios. Differential scanning calorimetry (DSC) and Fourier transform infrared (FT-IR) spectroscopic evaluations were carried out to assess compatibility between the drug and the excipients. The tablets were subjected to various pre- and post-compression evaluations, including in vitro drug release, in vitro bioadhesive strength, swelling and stability studies. Results: The results show that all the formulations satisfied Indian Pharmacopoeial specifications for tablet parameters. DSC and FT-IR data indicate there was no interaction between the drug and the excipients. Drug dissolution rate at pH 6.0 followed the rank order: HPMC)/NaCMC > HPMC/GG. There was increase in swelling index with time at 37°C. The combination of HPMC with NaCMC showed greater mucoadhesive strength and superior controlled drug release to the formulations prepared with GG polymer mixture. Furthermore, the release properties of the former in pH 6.0 buffer, as well as release mechanism (n values), were negligibly affected by ageing. Conclusion: This study indicates the possible use of suitable mixtures of natural and semi-synthetic cellulosic polymers for the preparation of clotrimazole mucoadhesive tablets for application as a vaginal controlled delivery system.
机译:目的:使用天然聚合物配制克罗咪唑生物粘附阴道片,以在感染部位提供长期治疗作用。方法:使用生物粘附性聚合物混合物:不同比例的羟丙基甲基纤维素/羧甲基纤维素钠(HPMC / NaCMC)和HPMC /瓜尔胶(GG)直接压片制备片剂。进行了差示扫描量热法(DSC)和傅立叶变换红外光谱(FT-IR)光谱评估,以评估药物与赋形剂之间的相容性。对片剂进行各种压缩前和压缩后评估,包括体外药物释放,体外生物粘附强度,溶胀和稳定性研究。结果:结果表明,所有制剂均满足印度药典对片剂参数的规定。 DSC和FT-IR数据表明药物与赋形剂之间没有相互作用。 pH 6.0时的药物溶出速率遵循等级顺序:HPMC)/ NaCMC> HPMC / GG。在37°C时,溶胀指数随时间增加。 HPMC与NaCMC的组合显示出比用GG聚合物混合物制备的制剂更高的粘膜粘附强度和更好的药物控制释放。此外,前者在pH 6.0缓冲液中的释放特性以及释放机理(n值)受老化影响很小。结论:这项研究表明,天然和半合成纤维素聚合物的合适混合物可用于制备克霉唑粘膜粘着片,用作阴道控制递送系统。

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